The impact of a change in antibacterial prophylaxis from ceftazidime to levofloxacin in allogeneic hematopoietic cell transplantation
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作者:
Guthrie, K. A.
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机构:Fred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Guthrie, K. A.
Yong, M.
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机构:Fred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Yong, M.
Frieze, D.
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Univ Washington, Sch Pharm, Seattle, WA 98195 USA
Univ Washington, Sch Med, Seattle, WA USAFred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Frieze, D.
[2
,3
]
Corey, L.
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Univ Washington, Sch Med, Seattle, WA USA
Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Inst, Seattle, WA 98109 USAFred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Corey, L.
[3
,4
]
Fredricks, D. N.
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Fred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Univ Washington, Sch Med, Seattle, WA USA
Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Inst, Seattle, WA 98109 USAFred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
Fredricks, D. N.
[1
,3
,4
]
机构:
[1] Fred Hutchinson Canc Res Ctr, Program Infect Dis, Div Clin Res, Seattle, WA 98109 USA
[2] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Seattle, WA USA
[4] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Inst, Seattle, WA 98109 USA
Antibiotic prophylaxis has been used during the initial phases of myeloablative hematopoietic cell transplantation (HCT) for more than two decades. However, the optimal regimen in terms of both cost and clinical effectiveness is unclear. We retrospectively compared the clinical and microbiological impact of a change in antibiotic prophylaxis practice from ceftazidime (n = 216 patients with HCT in 2000-2002) to levo. oxacin (n = 219 patients, August 2002-2005) in patients receiving myeloablative conditioning. Levo. oxacin prophylaxis was associated with fever and a change in antibiotics during neutropenia, but this strategy was not associated with any adverse outcomes. Patients receiving levo. oxacin had lower rates of significant bacteremia than did those receiving ceftazidime (day 100, 19.2 vs 29.6%, P = 0.02). The use of levo. oxacin was associated with lower antibiotic acquisition costs. There was no deleterious impact caused by levo. oxacin prophylaxis on survival, emergence of antibiotic resistance, detection of Clostridium difficile Ag in stool specimens, incidence of viridans group streptococcal bacteremia or Pseudomonas infections. There was a trend toward lower rates of bacteriuria, wound and bacterial respiratory infections in the levo. oxacin than in the ceftazidime group, but these differences were not statistically significant. These data support the use of levo. oxacin as prophylaxis in myeloablative allogeneic HCT when prophylaxis is used. Bone Marrow Transplantation (2010) 45, 675-681; doi:10.1038/bmt.2009.216; published online 31 August 2009